Allele Registry

Canonical Allele Identifier: PA2828115373

Gene: VMA21 HGNC NCBI

ClinVar Allele:

939463

ClinVar RCV:

RCV001208862

RCV003238319

ClinVar Variation:

939455

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350739.1:p.Ala130Thr	CA415271253 NM_001363810.1:c.388G>A